Operate as a Regulatory Affairs Manager in role which is based around providing strategic leadership for MAAâ€™s, lifecycle and development for products in the EMEA region for Oncology Biotech projects - If you wish to apply for this role send your CV to email@example.com or call Theo Moore or Matt Greig in the London office on +44 (0)207 801 3380 - or Marc Van de Voorde in our Swiss office, on +41 41 710 5100
Lead and provide regulatory strategy to submit scientific advice, achieve the successful application of a PIP and submit and validate an EU centralised MAA. Contact Theo Moore on +44 207 801 3380 or email me in confidence on firstname.lastname@example.org
In the short-term you will be leading RA development, Scientific advice, agency interaction and regulatory strategy - If you wish to apply for this role send your CV to email@example.com or call Theo Moore or Matt Greig in the London office on +44 (0)207 801 3380
With a focus on natural, long-term growth, this Blue-Chip organisation depends on the contributions of talented and committed professionals like you who are determined to drive through progress. In turn, they will make sure your work environment leaves you the space you need to attend to your personal goals, meet your family obligations, and pursue your professional development. Contact Theo Moore for more details on 0044 207 801 3380
Regulatory Affairs Associate Director. Therapeutically focused in Oncology. Permanent
Are you a senior Regulatory professional seeking to take the next step up in your Regulatory Affairs Career? If so, I have a fantastic permanent Regulatory Associate Director role available with a leading global pharmaceutical/R&D company located in London!
My client is looking for a Senior International Project Leader to lead and manage a team, taking responsibility a global project across in Rheumatology or Urology. The right candidate will have previous line management experience with at least 3 years experience in project management and clinical research. This is a great opportunity to join a growing pharmaceutical company which will offer a competitive salary and bonus, along with a professional and challenging environment.
Forward thinking client which is rated in the Top 10 of world Pharmaceutical companies - Excellent Benefits package which includes a great salary & benefits package - Strong pipeline with Oncology, CNS, Pain, Inflammation and Cardiovascular products in late phases of development - Location: Switzerland, Basel, NeuchÃ¢tel, Geneva,
In the first instance please call Matt or Theo on +44(0)207 801 3384 or +44 (0) 7918 195 166 or please send a full CV to Theo@advregulatory.com
This organisation has a healthy pipeline of early and late stage development projects and the regulatory department is uniquely set-up in such a way that you will have full project responsibility and leadership for your own Centralised registrations. If you wish to apply for this role send your CV to firstname.lastname@example.org or call Theo Moore or Matt Greig in the London office on +44 (0)207 801 3380 - or Marc Van de Voorde in our Swiss office, on +41 41 710 5100
Leading one or several cross functional study teams (and/or sub-teams) to deliver clinical research studies on time, within budget and with good quality in compliance with Regulatory Authorities regulations/guidelines and SOPs/WPs. Sharing best practices. Contributing to process improvement initiatives
PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her